EP2091507A1 - Haarkonditionierungszusammensetzungen - Google Patents
HaarkonditionierungszusammensetzungenInfo
- Publication number
- EP2091507A1 EP2091507A1 EP07822287A EP07822287A EP2091507A1 EP 2091507 A1 EP2091507 A1 EP 2091507A1 EP 07822287 A EP07822287 A EP 07822287A EP 07822287 A EP07822287 A EP 07822287A EP 2091507 A1 EP2091507 A1 EP 2091507A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- hair conditioning
- carbon atoms
- hydrophilic
- conditioning composition
- cationic surfactant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 59
- 230000003750 conditioning effect Effects 0.000 title claims abstract description 26
- 125000001424 substituent group Chemical group 0.000 claims abstract description 29
- 239000003093 cationic surfactant Substances 0.000 claims abstract description 24
- 239000000463 material Substances 0.000 claims abstract description 24
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 20
- 239000008365 aqueous carrier Substances 0.000 claims abstract description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 6
- 150000005215 alkyl ethers Chemical class 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 6
- -1 hydroxypropyl group Chemical group 0.000 claims description 5
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 claims description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 3
- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 claims description 3
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- VXAPDXVBDZRZKP-UHFFFAOYSA-N nitric acid phosphoric acid Chemical compound O[N+]([O-])=O.OP(O)(O)=O VXAPDXVBDZRZKP-UHFFFAOYSA-N 0.000 claims description 3
- 150000003839 salts Chemical group 0.000 claims description 3
- 229910021653 sulphate ion Inorganic materials 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 150000001450 anions Chemical class 0.000 claims description 2
- 229960000541 cetyl alcohol Drugs 0.000 claims description 2
- 229960000735 docosanol Drugs 0.000 claims description 2
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 claims description 2
- 229940012831 stearyl alcohol Drugs 0.000 claims description 2
- 239000004034 viscosity adjusting agent Substances 0.000 claims description 2
- 125000005313 fatty acid group Chemical group 0.000 claims 1
- 229920001296 polysiloxane Polymers 0.000 description 19
- 239000000839 emulsion Substances 0.000 description 16
- 239000002253 acid Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 125000002091 cationic group Chemical group 0.000 description 6
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 6
- 244000303965 Cyamopsis psoralioides Species 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 4
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 4
- YSJGOMATDFSEED-UHFFFAOYSA-M behentrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C YSJGOMATDFSEED-UHFFFAOYSA-M 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 4
- 229930182830 galactose Natural products 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000004530 micro-emulsion Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 240000008886 Ceratonia siliqua Species 0.000 description 2
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 229920002907 Guar gum Polymers 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000005233 alkylalcohol group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 229920003086 cellulose ether Polymers 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000004945 emulsification Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000000665 guar gum Substances 0.000 description 2
- 235000010417 guar gum Nutrition 0.000 description 2
- 229960002154 guar gum Drugs 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 229940049292 n-(3-(dimethylamino)propyl)octadecanamide Drugs 0.000 description 2
- KKBOOQDFOWZSDC-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCN(CC)CC KKBOOQDFOWZSDC-UHFFFAOYSA-N 0.000 description 2
- WWVIUVHFPSALDO-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCCN(C)C WWVIUVHFPSALDO-UHFFFAOYSA-N 0.000 description 2
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 150000005846 sugar alcohols Polymers 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- OMDQUFIYNPYJFM-XKDAHURESA-N (2r,3r,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4r,5s,6r)-4,5,6-trihydroxy-3-[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@H](O)[C@H](O)O1 OMDQUFIYNPYJFM-XKDAHURESA-N 0.000 description 1
- LPJKDVHMUUZHRY-KVVVOXFISA-N (z)-octadec-9-en-1-amine;hydrochloride Chemical compound Cl.CCCCCCCC\C=C/CCCCCCCCN LPJKDVHMUUZHRY-KVVVOXFISA-N 0.000 description 1
- HIAHPXLWIQVPMP-UHFFFAOYSA-N 20-aminoicosane-1,1-diol Chemical compound NCCCCCCCCCCCCCCCCCCCC(O)O HIAHPXLWIQVPMP-UHFFFAOYSA-N 0.000 description 1
- 240000006304 Brachychiton acerifolius Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920000926 Galactomannan Polymers 0.000 description 1
- 244000230012 Gleditsia triacanthos Species 0.000 description 1
- 235000013813 Gleditsia triacanthos Nutrition 0.000 description 1
- 239000005905 Hydrolysed protein Substances 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 229920000057 Mannan Polymers 0.000 description 1
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000012874 anionic emulsifier Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- TTZLKXKJIMOHHG-UHFFFAOYSA-M benzyl-decyl-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 TTZLKXKJIMOHHG-UHFFFAOYSA-M 0.000 description 1
- PXFDQFDPXWHEEP-UHFFFAOYSA-M benzyl-dimethyl-octylazanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(C)CC1=CC=CC=C1 PXFDQFDPXWHEEP-UHFFFAOYSA-M 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 1
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 229920013750 conditioning polymer Polymers 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- WLCFKPHMRNPAFZ-UHFFFAOYSA-M didodecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC WLCFKPHMRNPAFZ-UHFFFAOYSA-M 0.000 description 1
- NAPSCFZYZVSQHF-UHFFFAOYSA-N dimantine Chemical compound CCCCCCCCCCCCCCCCCCN(C)C NAPSCFZYZVSQHF-UHFFFAOYSA-N 0.000 description 1
- 229940008099 dimethicone Drugs 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000004665 fatty acids Chemical group 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- BUHXFUSLEBPCEB-UHFFFAOYSA-N icosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCN BUHXFUSLEBPCEB-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 238000002356 laser light scattering Methods 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 235000004213 low-fat Nutrition 0.000 description 1
- 125000000311 mannosyl group Chemical group C1([C@@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- KHPAAXRLVYMUHU-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)NCCN(CC)CC KHPAAXRLVYMUHU-UHFFFAOYSA-N 0.000 description 1
- UIUQXDQHAWBLOW-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]icosanamide Chemical compound CCCCCCCCCCCCCCCCCCCC(=O)NCCN(CC)CC UIUQXDQHAWBLOW-UHFFFAOYSA-N 0.000 description 1
- DYAVLIWAWOZKBI-UHFFFAOYSA-N n-[3-(diethylamino)propyl]hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCCN(CC)CC DYAVLIWAWOZKBI-UHFFFAOYSA-N 0.000 description 1
- OVCKOYOTKXBZKK-UHFFFAOYSA-N n-[3-(diethylamino)propyl]icosanamide Chemical compound CCCCCCCCCCCCCCCCCCCC(=O)NCCCN(CC)CC OVCKOYOTKXBZKK-UHFFFAOYSA-N 0.000 description 1
- KUIOQEAUQATWEY-UHFFFAOYSA-N n-[3-(diethylamino)propyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCCN(CC)CC KUIOQEAUQATWEY-UHFFFAOYSA-N 0.000 description 1
- BDHJUCZXTYXGCZ-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCCN(C)C BDHJUCZXTYXGCZ-UHFFFAOYSA-N 0.000 description 1
- SDGDJTPRANMWBS-UHFFFAOYSA-N n-icosyldocosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCCCC SDGDJTPRANMWBS-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 229940032160 stearamidoethyl diethylamine Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- YMBCJWGVCUEGHA-UHFFFAOYSA-M tetraethylammonium chloride Chemical compound [Cl-].CC[N+](CC)(CC)CC YMBCJWGVCUEGHA-UHFFFAOYSA-M 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
- AQZSPJRLCJSOED-UHFFFAOYSA-M trimethyl(octyl)azanium;chloride Chemical compound [Cl-].CCCCCCCC[N+](C)(C)C AQZSPJRLCJSOED-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- A61K8/737—Galactomannans, e.g. guar; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5422—Polymers characterized by specific structures/properties characterized by the charge nonionic
Definitions
- the present invention relates to hair conditioning compositions which comprise a polygalactomannan having hydrophilic and hydrophobic substituents .
- Hair conditioning compositions are typically applied to the hair immediately after shampooing and rinsing the hair.
- the conditioning composition is worked through the hair, and may then be left to penetrate the hair for a period of time before rinsing it from the hair with water.
- conditioning compositions have used a combination of cationic surfactants and fatty materials such as long chain fatty alcohols. This combination forms a lamellar gel phase which imparts a desirable viscosity to the product and deposits on the hair during use of the product to provide a conditioning benefit.
- thickeners which have been used for this purpose are nonionic cellulose ethers such as hydroxyethylcellulose .
- Hydrophobically-modified cellulose ethers such as cetyl hydroxyethylcellulose have also been used.
- Materials of this type are described in EP 412 705, EP 412 706 and EP 412 710 as providing a rheology very much like the gel-network structure of typical hair conditioners without the slimy feel associated with most polymeric thickeners, and without using a typical quaternary ammonium compound/fatty alcohol gel-network thickening system.
- a problem associated with the use of the above-described cellulosic thickeners is that it is difficult to obtain the right viscosity profile under different conditions of product usage. For example, a thick, creamy product viscosity is desirable to enable controlled pouring and product dosage onto the hair. A lower product viscosity is preferred to facilitate spreading of the product through the hair and rinsing, but not to the extent that the product is perceived to "disappear" into the hair.
- the inventors have found that this problem can be solved if a polygalactomannan having hydrophilic and hydrophobic substituents is used to thicken the hair conditioning composition .
- Substituted polygalactomannans of the above type have been proposed for the stabilisation of lathering compositions such as shower gels and shampoos in WO99/01105.
- the formulations in that publication are based on insoluble silicones and detergent surfactants.
- the invention provides a hair conditioning composition
- a hair conditioning composition comprising a cationic surfactant, a fatty material, a polygalactomannan having hydrophilic and hydrophobic substituents, and an aqueous carrier.
- the invention also provides the use of a polygalactomannan having hydrophilic and hydrophobic substituents as a viscosity modifier in a hair conditioning composition comprising cationic surfactant and fatty material.
- compositions according to the invention comprise one or more cationic surfactants which are cosmetically acceptable and suitable for topical application to the hair.
- Suitable cationic surfactants for use in compositions of the invention contain amino or quaternary ammonium hydrophilic moieties which are positively charged when dissolved in the composition.
- Suitable quaternary ammonium cationic surfactants correspond to the following general formula (I) :
- R 1 , R 2 , R 3 , and R 4 are each independently selected from (a) an aliphatic group of from 1 to 22 carbon atoms, or (b) an aromatic, alkoxy, polyoxyalkylene, alkylamido, hydroxyalkyl, aryl or alkylaryl group having up to 22 carbon atoms; and X is a salt-forming anion such as those selected from halogen, (e.g. chloride, bromide), acetate, citrate, lactate, glycolate, phosphate nitrate, sulphate, and alkylsulphate radicals.
- halogen e.g. chloride, bromide
- the aliphatic groups can contain, in addition to carbon and hydrogen atoms, ether linkages, and other groups such as amino groups.
- the longer chain aliphatic groups e.g., those of about 12 carbons, or higher, can be saturated or unsaturated.
- R 1 and R 2 are each independently selected from Ci6 to C 22 hydrocarbyl chains comprising at least one ester linkage in both R 1 and R 2 , and R 3 and R 4 are each independently selected from CH 3 and CH 2 CH 2 OH.
- R 1 and R 2 are each independently selected from C 1 6 to C 22 saturated or unsaturated, preferably saturated, chains, and R 3 and R 4 are each independently selected from CH 3 and CH 2 CH 2 OH, preferably CH 3 .
- R 1 is a Ci6 to C 22 alkyl chain and R 2 , R 3 and R 4 are each independently selected from CH 3 and CH 2 CH 2 OH, preferably CH 3 .
- quaternary ammonium cationic surfactants of general formula (I) are cetyltrimethylammonium chloride, behenyltrimethylammonium chloride (BTAC) , cetylpyridinium chloride, tetramethylammonium chloride, tetraethylammonium chloride, octyltrimethylammonium chloride, dodecyltrimethylammonium chloride, hexadecyltrimethylammonium chloride, octyldimethylbenzylammonium chloride, decyldimethylbenzylammonium chloride, stearyldimethylbenzylammonium chloride, didodecyldimethylammonium chloride, dioctadecyldimethylammonium chloride, tallowtrimethylammonium chloride, cocotrimethylammonium chloride, dipalmitoylethyldimethylammonium chloride, PEG-2
- Particularly preferred quaternary ammonium cationic surfactants for use in the invention are cetyltrimethylammonium chloride, available commercially, for example as GENAMIN CTAC, ex Hoechst Celanese and Arquad 16/29 supplied by Akzo Nobel, and behenyltrimethylammonium chloride (BTAC) such as Genamin KDM-P supplied by Clariant. Mixtures of any of the foregoing materials may also be suitable .
- Salts of primary, secondary, and tertiary fatty amines are also suitable cationic surfactants for use in the invention.
- the alkyl groups of such amines preferably have from about 12 to about 22 carbon atoms, and can be substituted or unsubstituted. These amines are typically used in combination with an acid to provide the cationic species.
- a preferred class of amine corresponds to the following general formula (II):
- R 1 is a fatty acid chain containing from 12 to 22 carbon atoms
- R 2 is an alkylene group containing from one to four carbon atoms
- R 3 and R 4 are, independently, an alkyl group having from one to four carbon atoms .
- Suitable materials of general formula (II) are stearamidopropyldimethylamine, stearamidopropyldiethylamine, stearamidoethyldiethylamine, stearamidoethy1dimethylamine, palmitamidopropyldimethylamine, palmitamidopropyldiethylamine, palmitamidoethyldiethylamine, palmitamidoethyldimethylamine, behenamidopropyldimethy1amine, behenamidopropyldiethylamine, behenamidoethyldiethylamine, behenamidoethyldimethylamine, arachidamidopropyldimethy1amine, arachidamidopropyldiethylamine, arachidamidoethyldiethylamine, arachidamidoethy1dimethylamine, and diethylaminoethy
- dimethylstearamine dimethylsoyamine, soyamine, myristylamine, tridecylamine, ethylstearylamine, N- tallowpropane diamine, ethoxylated (with 5 moles of ethylene oxide) stearylamine, dihydroxyethylstearylamine, and arachidyl behenylamine .
- Particularly preferred is stearamidopropyldimethylamine .
- the acid used to provide the cationic species can be any organic acid or mineral acid of sufficient acid strength to neutralise a free amine nitrogen.
- Such acids include hydrochloric acid, sulphuric acid, nitric acid, phosphoric acid, lactic acid, citric acid, tartaric acid, acetic acid, gluconic acid, glycolic acid and propionic acid, or combinations thereof.
- a sufficient amount of acid is added to neutralise the amidoamine compound and to adjust the final pH of the composition to within a range of from about 2.5 to about 6, preferably in a pH range of from about 3 to about 5.
- the molar ratio of protonatable amine groups to H + from the acid is preferably from about 1:0.3 to 1:1.2, and more preferably from about 1:0.5 to about 1:1.1. Mixtures of any of the above-described cationic surfactants may also be suitable.
- the level of cationic surfactant preferably ranges from 0.1 to 10%, more preferably 0.2 to 5%, most preferably 0.25 to 4% by total weight of cationic surfactant based on the total weight of the composition.
- compositions of the invention comprise a fatty material.
- the fatty material together with the cationic surfactant and an aqueous carrier, forms a lamellar gel phase which is suitable for providing various hair conditioning attributes.
- fatty material is meant a compound having the general formula R-X, wherein R is an aliphatic carbon chain and X is a functional group (e.g. alcohol, acid, or derivative).
- R is preferably a fully saturated aliphatic carbon chain comprising from 8 to 30 carbon atoms, more preferably from 16 to 22 carbon atoms.
- X is preferably an alcohol group.
- the fatty material is selected from cetyl alcohol, stearyl alcohol, behenyl alcohol, and mixtures thereof .
- the level of fatty material in conditioners of the invention suitably ranges from 0.01 to 15%, preferably from 0.1 to 10%, and more preferably from 0.1 to 5% by total weight fatty material based on the total weight of the composition.
- the weight ratio of cationic surfactant to fatty material is suitably from 10:1 to 1:10, preferably from 4:1 to 1:8, more preferably from 1:1 to 1:7.
- Polygalactomannans are polysaccharides composed principally of galactose and mannose units and are usually found in the endosperm of certain leguminous seeds such as guar, locust bean, honey locust, flame tree and the like.
- Guar gum for example, is composed mostly of a galactomannan with essentially is a straight chain mannan with single membered galactose branches. The ratio of galactose to mannose in the guar polymer is 1:2.
- Locust bean gum is a polygalactomannan gum of similar molecular structure in which the ratio of galactose to mannose is 1:4.
- Guar and locust bean gums are preferred sources of the polygalactomannans, principally because of their commercial availability. Guar gum is a most preferred source.
- substituted polygalactomannans for use in compositions of the invention (hereinafter referred to as "substituted polygalactomannans”) contain hydrophilic substituents and hydrophobic substituents.
- the substituted polygalactomannan is derived from a polygalactomannan having a molecular weight of from 50,000 to 1,600,000, depending on the origin of the polygalactomannan .
- Suitable substituted polygalactomannans have a total molar substitution of greater than 0.7. Preferably the total molar substitution ranges from 0.9 to 2.01. By “molar substitution” is meant the average number of moles of substituents on each anhydroglycosidic unit of the polygalactomannan .
- Suitable substituted polygalactomannans contain an average of from 0.7 to 4 hydrophilic substituents per anhydroglycosidic unit.
- Preferred substituted polygalactomannans contain an average of from 0.9 to 2 hydrophilic substituents per anhydroglycosidic unit.
- Suitable substituted polygalactomannans contain an average of from 0.0001 to 0.02 hydrophobic substituents per anhydroglycosidic unit.
- Preferred substituted polygalactomannans contain an average of from 0.0005 to 0.01 hydrophobic substituents per anhydroglycosidic unit.
- the molar ratio of hydrophilic substituents to hydrophobic substituents ranges from 35:1 to 40,000:1.
- the molar ratio ranges from 90:1 to 4000:1.
- the hydrophilic substituents may suitably be selected from C 2 -C 4 alkyl groups, C 2 -C 4 hydroxyalkyl groups, carboxymethyl, amino and carboxylic groups.
- the hydrophilic substituents are C2-C4 hydroxyalkyl groups, most preferably hydroxypropyl groups. Mixtures of any of the above hydrophilic substituents may also be suitable.
- the hydrophobic substituents may suitably be chosen from linear or branched alkyl and alkenyl groups containing from 10 to 32 carbon atoms, more preferably from 14 to 28 carbon atoms.
- the alkyl or alkenyl groups can be substituted with one or more hydroxyl groups. Mixtures of any of the above hydrophobic substituents may also be suitable.
- hydrophilic and hydrophobic substituents can either be linked directly via a carbon-carbon bond to the anhydroglycoside unit, or can be linked via an ether, urethane, ester, amide or acyl bond and preferably via an ether bond.
- Preferred substituted polygalactomannans for use in the invention are poly (alkyl ethers) of polygalactomannans having hydrophilic and hydrophobic alkyl ether substituents respectively.
- Examples of such materials are poly (alkyl ethers) of polygalactomannans in which the hydrophilic substituent is HOR 1 -, in which R 1 is an alkylene group having two to four carbon atoms and in which the OH group is on the carbon atom beta to the ether group, and the hydrophobic substituent is chosen from R 2 , HOR 3 , and R 4 O-CH 2 CH(OH)-CH 2 -, in which R 2 is an alkyl group which contains 10 to 32 carbon atoms, R 3 is an alkylene group which contains 10 to 32 carbon atoms having the OH group on the carbon atom beta to the ether group and R 4 is an alkyl group having from 7 to 29 carbon atoms.
- the hydrophilic substituent is HOR 1 -
- R 1 is an alkylene group having two to four carbon atoms and in which the OH group is on the carbon atom beta to the ether group
- the hydrophobic substituent is chosen from R 2 , HOR 3 , and
- Preferred examples of such materials are poly (alkyl ethers) of polygalactomannans in which the hydrophilic substituent is the hydroxypropyl group and the hydrophobic substituent is a linear alkyl group containing from 14 to 28 carbon atoms or a mixture of such alkyls.
- substituted polygalactomannans suitable for use in compositions of the invention are guar gums sold under the name Esaflor HM 22 by the company Lamberti or under the name Jaguar XC 95-3 by the company Rh ⁇ ne-Poulenc .
- the level of substituted polygalactomannan in conditioners of the invention suitably ranges from 0.001 to 10%, preferably from 0.005 to 5%, and more preferably from 0.01 to 2% by total weight substituted polygalactomannan based on the total weight of the composition.
- the conditioning composition of the present invention comprises an aqueous carrier.
- Suitable aqueous carriers are water and water solutions of lower alkyl alcohols and polyhydric alcohols.
- Suitable lower alkyl alcohols are monohydric alcohols having 1 to 6 carbons, preferably ethanol and isopropanol .
- Suitable polyhydric alcohols are propylene glycol, hexylene glycol, glycerin, and propanediol.
- the aqueous carrier is substantially water.
- compositions according to the invention comprise at least 60%, preferably at least 65%, more preferably at least 70% water by weight based on the total weight of the composition .
- compositions of the invention may comprise further conditioning agents to optimise wet and dry conditioning benefits .
- Particularly preferred further conditioning agents are silicone emulsions.
- Suitable silicone emulsions include those formed from silicones such as polydiorganosiloxanes, in particular polydimethylsiloxanes which have the CTFA designation dimethicone, polydimethyl siloxanes having hydroxyl end groups which have the CTFA designation dimethiconol, and amino-functional polydimethyl siloxanes which have the CTFA designation amodimethicone .
- the emulsion droplets may typically have a Sauter mean droplet diameter (D 3 , 2) in the composition of the invention ranging from 0.01 to 20 micrometer, more preferably from 0.2 to 10 micrometer.
- D 3 Sauter mean droplet diameter
- a suitable method for measuring the Sauter mean droplet diameter (D 3 , 2 ) is by laser light scattering using an instrument such as a Malvern Mastersizer.
- Suitable silicone emulsions for use in compositions of the invention are available from suppliers of silicones such as Dow Corning and GE Silicones. The use of such pre-formed silicone emulsions is preferred for ease of processing and control of silicone particle size.
- Such pre-formed silicone emulsions will typically additionally comprise a suitable emulsifier such as an anionic or nonionic emulsifier, or mixture thereof, and may be prepared by a chemical emulsification process such as emulsion polymerisation, or by mechanical emulsification using a high shear mixer.
- Preformed silicone emulsions having a Sauter mean droplet diameter (D 3 , 2 ) of less than 0.15 micrometers are generally termed microemulsions .
- Suitable pre-formed silicone emulsions include emulsions DC2-1766, DC2-1784, DC-1785, DC-1786, DC-1788 and microemulsions DC2-1865 and DC2-1870, all available from Dow Corning. These are all emulsions/microemulsions of dimethiconol . Also suitable are amodimethicone emulsions such as DC939 (from Dow Corning) and SME253 (from GE Silicones) .
- silicone emulsions in which certain types of surface active block copolymers of a high molecular weight have been blended with the silicone emulsion droplets, as described for example in WO03/094874.
- the silicone emulsion droplets are preferably formed from polydiorganosiloxanes such as those described above.
- One preferred form of the surface active block copolymer is according to the following formula:
- Silicone will generally be present in a composition of the invention at levels of from 0.05 to 10%, preferably 0.05 to 5%, more preferably from 0.5 to 2% by total weight of silicone based on the total weight of the composition.
- compositions according to the invention may also incorporate other cosmetically suitable ingredients, preferably at a level of 2% by weight or less.
- Suitable ingredients include: preservatives, colouring agents, chelating agents, antioxidants, fragrances, antimicrobials, antidandruff agents, cationic conditioning polymers, styling ingredients, sunscreens, proteins and hydrolysed proteins.
- compositions of the invention may be used by applying them to wet hair, typically hair which has been shampooed and then rinsed with water.
- the composition is applied to the hair and then worked through the hair.
- the composition is then left to penetrate the hair for a period of about one to three minutes before rinsing it from the hair with water.
- a series of hair conditioning compositions were prepared having ingredients as shown in the following Table 1:
- compositions were evaluated for their viscosity behaviour under varying conditions of shear stress.
- compositions according to the invention have a superior viscosity profile under conditions of low and high shear, when compared to Comparative Examples (A, B, C, D) with the same surfactant base .
- Compositions according to the invention have a desirable thick viscosity at low shear, which does not break down too rapidly at high shear. If viscosity breakdown is too rapid at high shear (for example as shown in Comparative Example B) , the conditioner will be perceived to "disappear" into the hair when it is spread through the hair by the consumer
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0624132.7A GB0624132D0 (en) | 2006-12-02 | 2006-12-02 | Hair conditioning compositions |
PCT/EP2007/061971 WO2008064976A1 (en) | 2006-12-02 | 2007-11-07 | Hair conditioning compositions |
Publications (3)
Publication Number | Publication Date |
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EP2091507A1 true EP2091507A1 (de) | 2009-08-26 |
EP2091507B1 EP2091507B1 (de) | 2015-03-25 |
EP2091507B2 EP2091507B2 (de) | 2018-08-01 |
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EP07822287.4A Active EP2091507B2 (de) | 2006-12-02 | 2007-11-07 | Haarkonditionierungszusammensetzungen |
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US (1) | US20100135947A1 (de) |
EP (1) | EP2091507B2 (de) |
JP (1) | JP5745223B2 (de) |
CN (1) | CN101583343A (de) |
BR (1) | BRPI0717698B1 (de) |
ES (1) | ES2540060T3 (de) |
GB (1) | GB0624132D0 (de) |
MX (1) | MX348260B (de) |
RU (1) | RU2443409C2 (de) |
WO (1) | WO2008064976A1 (de) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
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AU2009262207A1 (en) * | 2008-06-25 | 2009-12-30 | The Procter & Gamble Company | Hair conditioning composition containing behenyl trimethyl ammonium methosulfate, and having higher yield point |
CN103998100A (zh) * | 2011-12-20 | 2014-08-20 | 荷兰联合利华有限公司 | 生产结构化液体的方法以及结构化液体 |
BR112016007572A8 (pt) * | 2013-10-07 | 2020-03-03 | Hercules Inc | composição, composição de fixador para os cabelos e método para a produção uma poligalactomanana dihidroxipropil-substituída |
CN107049830A (zh) * | 2017-05-04 | 2017-08-18 | 上海章华保健化妆品有限公司 | 一种高稳定性护发素及其制备方法 |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
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PH16210A (en) * | 1980-03-10 | 1983-08-05 | Procter & Gamble | Hair conditioning compositions |
US4870167A (en) * | 1987-03-02 | 1989-09-26 | Hi-Tek Polymers, Inc. | Hydrophobically modified non-ionic polygalactomannan ethers |
JPH0474108A (ja) * | 1990-05-16 | 1992-03-09 | Shin Etsu Chem Co Ltd | 化粧料 |
FR2739282B1 (fr) * | 1995-09-29 | 1997-10-31 | Oreal | Composition topique contenant un polymere a squelette polysiloxanique a greffons non-silicones et un polymere amphiphile a chaine grasse |
FR2765479B1 (fr) * | 1997-07-02 | 1999-10-29 | Oreal | Composition lavantes et conditionnantes a base de silicone et de gomme de galactomannane hydrophobe |
FR2804015B1 (fr) * | 2000-01-21 | 2005-12-23 | Oreal | Nanoemulsion contenant des lipides amphiphiles et un polymere non ionique et utilisations |
FR2805990B1 (fr) * | 2000-03-07 | 2003-04-11 | Oreal | Composition capillaire epaissie comprenant un polymere fixant et un compose pulverulent |
JP2003160446A (ja) * | 2001-11-28 | 2003-06-03 | Kose Corp | ヘアコンディショニング組成物 |
FR2841466B1 (fr) * | 2002-06-28 | 2005-12-30 | Oreal | Composition cosmetique comprenant une silicone quaternaire et un alcool gras liquide et procede de traitement cosmetique |
US20040247550A1 (en) * | 2003-06-06 | 2004-12-09 | The Procter & Gamble Company | Hair or skin conditioning composition comprising hydrophobically modified cationic thickening polymer |
US7390478B2 (en) * | 2004-02-23 | 2008-06-24 | Sebastian International, Inc. | Hair thickening composition and method |
BRPI0513608A (pt) * | 2004-07-27 | 2008-05-13 | Unilever Nv | composição para o cuidado dos cabelos, processo para a preparação de uma composição para o cuidado dos cabelos e método para o tratamento dos cabelos |
CA2598064A1 (en) | 2005-02-25 | 2006-09-08 | The Procter & Gamble Company | Hair or skin conditioning compositions comprising hydrophobically modified amido silicone copolyol |
US20060210509A1 (en) * | 2005-03-21 | 2006-09-21 | Johnson Andress K | Hair conditioner |
WO2007065537A1 (en) * | 2005-12-08 | 2007-06-14 | Unilever Plc | Shampoo compositions containing a combination of cationic polymers |
FR2895251B1 (fr) * | 2005-12-22 | 2008-04-04 | Oreal | Composition cosmetique comprenant au moins un poly(vinyllactame) cationique, au moins un alcool gras et au moins une silicone aminee, procede de traitement cosmetique et utilisation de la composition |
US8936779B2 (en) * | 2005-12-22 | 2015-01-20 | L'oreal | Cosmetic composition comprising at least one cationic poly(vinyllactam), at least one fatty alcohol and at least one amino silicone, cosmetic process and use of the composition |
-
2006
- 2006-12-02 GB GBGB0624132.7A patent/GB0624132D0/en not_active Ceased
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2007
- 2007-11-07 MX MX2009005748A patent/MX348260B/es active IP Right Grant
- 2007-11-07 EP EP07822287.4A patent/EP2091507B2/de active Active
- 2007-11-07 RU RU2009125234/15A patent/RU2443409C2/ru active
- 2007-11-07 ES ES07822287.4T patent/ES2540060T3/es active Active
- 2007-11-07 US US12/516,811 patent/US20100135947A1/en not_active Abandoned
- 2007-11-07 BR BRPI0717698A patent/BRPI0717698B1/pt active IP Right Grant
- 2007-11-07 CN CNA2007800444392A patent/CN101583343A/zh active Pending
- 2007-11-07 WO PCT/EP2007/061971 patent/WO2008064976A1/en active Application Filing
- 2007-11-07 JP JP2009538668A patent/JP5745223B2/ja active Active
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BRPI0717698A2 (pt) | 2013-10-29 |
CN101583343A (zh) | 2009-11-18 |
BRPI0717698B1 (pt) | 2016-01-19 |
MX348260B (es) | 2017-06-05 |
RU2009125234A (ru) | 2011-01-10 |
EP2091507B2 (de) | 2018-08-01 |
RU2443409C2 (ru) | 2012-02-27 |
GB0624132D0 (en) | 2007-01-10 |
EP2091507B1 (de) | 2015-03-25 |
ES2540060T3 (es) | 2015-07-08 |
JP5745223B2 (ja) | 2015-07-08 |
US20100135947A1 (en) | 2010-06-03 |
MX2009005748A (es) | 2009-07-14 |
JP2010511599A (ja) | 2010-04-15 |
WO2008064976A1 (en) | 2008-06-05 |
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